A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610409



Internal ID16397818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12949552..13038271hg38UCSC Ensembl
Innerchr8:12807061..12895780hg19UCSC Ensembl
Innerchr8:12851432..12940151hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3888720
hg1988720
hg1888720
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155982
SamplesHGDP01172
Known GenesKIAA1456
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610409
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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